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2-bromo-1-(2-chloroethoxy)-4-methoxybenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121767-80-4

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121767-80-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121767-80-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,7,6 and 7 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 121767-80:
(8*1)+(7*2)+(6*1)+(5*7)+(4*6)+(3*7)+(2*8)+(1*0)=124
124 % 10 = 4
So 121767-80-4 is a valid CAS Registry Number.

121767-80-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-1-(2-chloroethoxy)-4-methoxybenzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:121767-80-4 SDS

121767-80-4Relevant academic research and scientific papers

ENDOTHELIN RECEPTOR ANTAGONISTS

-

Page column 20, (2008/06/13)

Novel pyrroles, pyrazoles and triazoles, pharmaceutical compositions containing these compounds and their use as endothelin receptor antagonists are described.

ENDOTHELIN RECEPTOR ANTAGONISTS

-

, (2008/06/13)

Novel pyrroles, pyrazoles and triazoles, pharmaceutical compositions containing these compounds and their use as endothelin receptor antagonists are described.

Relevance of Conformational Constraints to the Regioselective Lithiation of Aromatic Diethers. Application to the Convenient Construction of the DEF Tricyclic Subunit of the Austalides

Paquette, Leo A.,Schulze, Matthias M.,Bolin, David G.

, p. 2043 - 2051 (2007/10/02)

The lithiation of 29 and 30 is shown to occur at all three sites with a dissimilar kinetic preference.For the dihydrofuran, reaction at the proton labeled Hβ' operates predominantly; in the dihydropyran example, Hα is the favored sit

The Synthesis of 5-Substituted 2,3-Dihydrobenzofurans

Alabaster, Ramon J.,Cottrell, Ian F.,Marley, Hugh,Wright, Stanley H. B.

, p. 950 - 952 (2007/10/02)

The preparation of 2,3-dihydrobenzofurans 6 from 2-(2-bromophenoxy)ethyl chlorides 3 by reaction with magnesium in a development of the Parham cyclialkylation reaction is described.A high yielding procedure using phase-transfer catalysis has also been developed for the preparation of the intermediate chloroethyl ethers 3 from bromophenols 2.The 5-hydroxy derivative 15 may be obtained from 2,3-dihydrobenzofuran (6a) by reaction with electrophilic reagents followed by oxidation.

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